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RELIEEV Uterine Manipulator Injector (CUMI 5.0)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240364
510(k) Type
Traditional
Applicant
LI Medical Corporation Ltd.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
10/16/2024
Days to Decision
253 days
Submission Type
Summary

RELIEEV Uterine Manipulator Injector (CUMI 5.0)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240364
510(k) Type
Traditional
Applicant
LI Medical Corporation Ltd.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
10/16/2024
Days to Decision
253 days
Submission Type
Summary